| Product NDC: | 64893-001 |
| Proprietary Name: | Binaca Anticavity Flouride Peppermint |
| Non Proprietary Name: | SODIUM MONOFLUOROPHOSPHATE |
| Active Ingredient(s): | .76 g/100g & nbsp; SODIUM MONOFLUOROPHOSPHATE |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 64893-001 |
| Labeler Name: | Dr. Fresh, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100504 |
| Package NDC: | 64893-001-24 |
| Package Description: | 24 g in 1 TUBE (64893-001-24) |
| NDC Code | 64893-001-24 |
| Proprietary Name | Binaca Anticavity Flouride Peppermint |
| Package Description | 24 g in 1 TUBE (64893-001-24) |
| Product NDC | 64893-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SODIUM MONOFLUOROPHOSPHATE |
| Dosage Form Name | PASTE, DENTIFRICE |
| Route Name | DENTAL |
| Start Marketing Date | 20100504 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Dr. Fresh, Inc |
| Substance Name | SODIUM MONOFLUOROPHOSPHATE |
| Strength Number | .76 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |